Description
General Responsibilities:- Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects
- Travels to field sites to monitor studies
- Reviews study protocols, reports and manuscripts. Contribute technical and clinical operations expertise for these documents
- Works with Data Management and Biostatistical staff on the design of documents and processes for the collection of study data from participating sites
- Assists with the coordination of training and certification of study site personnel
- Manages material logistics for the studies
- Participates in Project Team Meetings
Requirements:
- B.S. or M.S. in Biology, Chemistry, Molecular Biology or related discipline
- 3-6 years of relevant clinical research experience
- Strong science/lab background required
- Field monitoring experience required
- Medical device or diagnostic clinical research experience preferred but not required
- Travel: 15-35 % during occasional peak periods
To find out more about Real please visit www.realstaffing.com